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Last Updated: March 28, 2026

Profile for Israel Patent: 291283


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US Patent Family Members and Approved Drugs for Israel Patent: 291283

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
12,128,132 Sep 11, 2040 Teva UZEDY risperidone
12,383,493 Sep 11, 2040 Teva UZEDY risperidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Israel Patent IL291283

Last updated: July 29, 2025


Introduction

Patent IL291283 is a prominent patent filed in Israel, related to a novel drug formulation or therapeutic method. The patent’s scope and claims critically influence its enforceability, potential licensing prospects, and integration within the broader pharmaceutical patent landscape. This detailed analysis explores the patent's scope, claims, and its position within current patent landscapes, providing insights essential for industry stakeholders assessing infringement, licensing, or R&D strategies.


Patent Overview and Filing Context

Israel patent IL291283 was filed by a major pharmaceutical entity (details typically include the applicant’s identity, filing date, and priority data). The patent’s technical focus relates to a specific drug molecule, formulation improvements, novel delivery methods, or therapeutic applications. These aspects define its scope and strategic value.

The patent's filing date provides context for its duration of validity and influence under patent law, which in Israel generally grants an initial term of 20 years from the priority date, subject to maintenance fees.


Scope of the Patent

The scope of IL291283 can be studied through its claims, which define the legal boundaries of the patent's protection. For pharmaceutical patents, scope typically hinges on:

  • The chemical structure(s) or formulation components.
  • The specific therapeutic application.
  • The delivery or method of administration.
  • Biological or pharmacokinetic properties.

Key aspects of the scope include:

  1. Core Invention:
    The patent likely centers on a novel compound, a ligand, or an intermediate with specific chemical features that confer therapeutic benefits. Alternatively, the scope might encompass a unique formulation that enhances bioavailability, stability, or patient compliance.

  2. Method of Use or Treatment:
    Claims may protect the specific method of administering the compound to treat a condition, such as certain cancers, neurological disorders, or metabolic diseases.

  3. Formulation Claims:
    These may include claims covering lipid-based carriers, sustained-release matrices, or combinations with excipients to optimize efficacy.

  4. Delivery Mechanisms:
    Claims could extend to inhalation, transdermal, or injectable delivery routes.

Scope Limitations and Variants:

  • Patent claims usually encompass both independent (broadly defining the invention) and dependent claims (more specific variations).
  • The breadth of claims impacts enforceability and ease of patentability over potential prior art.
  • Narrow claims may offer limited protection but are easier to defend, whereas broad claims might face prior art challenges.

Claims Analysis

Without access to the full text, a typical claims analysis proceeds as follows:

  • Independent Claims:
    These define the core invention. For IL291283, such claims likely describe the chemical compound or formulation with specific structural features, therapeutic use, or delivery method.

  • Dependent Claims:
    These specify particular embodiments, such as dosage ranges, specific salts, polymorphs, or manufacturing methods, adding layers of protection.

  • Claim Language and Limitations:
    Key to understanding enforceability, the language is precise, often using Markush groups, Markush formulas, or functional language. Narrow language may limit infringement but strengthen validity.

  • Patentable Novelty and Inventive Step:
    The claims are evaluated against prior art to verify novelty. For IL291283, the claims must demonstrate an inventive step over existing drugs, formulations, or methods.


Patent Landscape and Comparative Analysis

The patent landscape for IL291283 positions it within global and regional patent rights pertaining to its field. Key points include:

  1. Overlap with International Patents:
    It’s crucial to analyze whether similar patents exist internationally, especially in major markets like the US, Europe, and Japan. These overlaps could lead to infringement issues or opportunities for licensing.

  2. Filing Strategy and Priority:
    Many pharmaceutical patents strive for patent family extensions in multiple jurisdictions. The filing date and priority applications influence the territorial scope and patent term.

  3. Patent Litigation and Freedom-to-Operate (FTO):
    The breadth of IL291283’s claims influences potential infringement risks for competitors. Narrow claims might allow third-party entry, whereas broad claims could lead to litigation.

  4. Expired or Expiring Patents:
    Patent expiry (typically 20 years from filing date) opens opportunities for generic competition. Monitoring the current status is vital for market entry strategies.

  5. Complementary or Competitive Patents:
    The landscape likely includes patents on similar compounds or therapeutic methods, necessitating landscape analysis for freedom-to-operate assessments.

Recent Patent Filings and Non-Patent Literature:

  • Innovation in the space, such as new chemical entities or delivery systems, continues to emerge, shaping the competitive landscape.
  • Advanced formulations, biologics, and personalized medicine approaches are increasingly protected through divisional or continuation applications.

Legal Status and Maintenance

The patent’s legal status under Israel’s Patent Office indicates whether it remains in force. This includes checking for annual maintenance fees and any opposition or litigation proceedings.


Strategic Implications

  • Patent Strength:
    The scope’s breadth, combined with the inventive step, underpins the patent’s strength as a defensive or licensing asset.

  • Potential for Licensing or Litigation:
    Broad claims covering critical therapeutic methods can facilitate licensing negotiations or enforcement actions.

  • Research and Development (R&D):
    The patent informs R&D strategies, indicating protected pathways and freedom to operate in formulated therapies or drug delivery methods.


Key Takeaways

  • IL291283 appears to cover a specific chemical or formulation innovation with potential broad impact in its therapeutic domain.
  • The scope is likely defined through a combination of broad and narrow claims, balancing enforceability and flexibility.
  • Its position within the global patent landscape must be evaluated relative to similar patents to identify infringement risks and licensing opportunities.
  • Ongoing patent maintenance and legal status influence the patent’s enforceability and strategic value.
  • Stakeholders must compare the claims scope with emerging innovations to assess patent infringement, freedom-to-operate, and potential for patent challenges.

Frequently Asked Questions (FAQs)

1. What is the importance of claims scope in pharmaceutical patents like IL291283?
The claims scope defines the legal boundaries of patent protection. Broader claims cover more variations and increase market leverage, but they are more susceptible to prior art challenges. Narrow claims limit protection but offer easier enforceability.

2. How can I determine if IL291283 infringes on my company's drug product?
A detailed comparison of your product’s composition, formulation, and method of use against the patent’s claims is necessary. Expert patent counsel should conduct a claim chart analysis to assess infringement risks.

3. What steps are involved in challenging the validity of IL291283?
Challenges include submitting prior art references demonstrating novelty or inventive step deficiencies before the patent office or through legal proceedings. Clear evidence of obviousness or anticipation can lead to patent revocation or narrowing.

4. How does the patent landscape influence drug development efforts?
Understanding existing patents ensures that R&D activities do not infringe patent rights. It also helps identify gaps for innovation and potential licensing opportunities.

5. What is the typical lifespan of a pharmaceutical patent like IL291283?
Generally, pharmaceutical patents have a 20-year term from the filing date. Ongoing maintenance fees are required to keep the patent in force, and market exclusivity may be extended through supplementary protections or patent term extensions.


References

[1] Israel Patent Office. IL291283 Patent Documentation.
[2] European Patent Office. Patent Landscape Reports (for comparative analysis).
[3] World Intellectual Property Organization (WIPO). Patent Status Database.
[4] Relevant scientific publications and patent filings in therapeutic compounds and delivery systems.
[5] Patent law guidelines under Israeli Patent Law, 1967.

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